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The IntelliVue MX430 patient monitor offers a • Previous Screen function provides access to the
flexible and modular monitoring solution, designed most recently used screens including the last three
to suit a broad spectrum of needs. The monitor can modified screens.
be connected to the Philips Multi-Measurement • Ventilation, hemodynamic, and oxygenation
Module (MMS) family with its extensions to extend calculations.
its functionality with plug-and-play convenience. • Gases can be displayed in kPa or mmHg.
Dedicated configurations are available for the • Pressure measurements can be displayed in kPa or
general care environment. mmHg.
• Temperature, height, and weight can be configured
Features either in metric or imperial units.
• Intuitive user interface. • Patient data management with tabular and graphic
• Simple menu hierarchy gives fast access to all basic trends.
monitoring tasks. • User or case-specific profiles enable rapid case
• Screen layouts are easily adjustable, allowing turnover.
flexible display of measurement information. • Patented automatic alarm limits help clinicians
provide care more efficiently.
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• Event Surveillance including for automatic detection of patient status The monitors are available as standalone or networked solutions.
deterioration. The monitor’s modular design allows new capabilities to be added in
• Bed-to-bed overview provides clinicians with an overview of all the the future as monitoring requirements change. This upgradability gives
patient beds in their care. the security of knowing that the monitor can be enhanced and updated
• Choice of input devices: Touchscreen, trackball, mouse, keyboard, or as practices and technologies advance, protecting long-term
barcode reader. investments.
• Built-in Recorder.
• Graphical measurement window shows which measurements are Main Components
being measured by which device, making it easier to resolve
measurement label conflicts. Display
• Timers application allows you to set timers to notify you when a The monitor has a color 12 inch LCD TFT display, providing high
specific time period has expired. resolution waveform and data presentation.
• The monitor can be configured to automatically adapt the screen The monitor integrates the display and the processing unit into one
brightness to the ambient light conditions.The range within which this device. One external display1 - providing an adaptive duplicate-image of
adaption is made is determined by the setting made with the the primary display - can be connected to a built-in DVI-I port.
brightness SmartKey.
• Integrated carrying handle. User Interface
The color Graphical-User-Interface is designed for fast and intuitive
Indications for Use operation, and ensures that clinicians quickly feel at ease using the
The monitor is indicated for use by health care professionals whenever monitor.
there is a need for monitoring the physiological parameters of patients. SmartKeys with intuitive icons allow monitoring tasks to be performed
The monitor is intended to be used for monitoring and recording of, quickly and easily, directly on the monitor screen.
and to generate alarms for, multiple physiological parameters of adults, Waves and numerics are color-coded.
pediatrics, and neonates. The monitor is intended for use by trained The monitor displays up to six waves simultaneously. For 12-lead ECG
healthcare professionals in a hospital environment. monitoring it can display 12 real-time ECG waves, with a rhythm strip.
The monitor is additionally intended for use in transport situations Flexible screen layout allows optimal use of the available display space,
within hospital environments. for example, waves can be overlapped or wave size can adjust
The monitor is only for use on one patient at a time. It is not intended dynamically depending on the number of waves configured for the
for home use. Not a therapeutic device. The monitor is for space.
prescription use only. The Basic Help provides on-screen operating help, explaining INOP
and alarm messages.
Rx only: U.S. Federal Law restricts this device to sale by or on the
order of a physician. Touchscreen Operation
The monitor is supplied as standard with a resistive touchscreen
The ECG measurement is intended to be used for diagnostic recording display.
of rhythm and detailed morphology of complex cardiac complexes
(according to AAMI EC 11). Input Devices
The Integrated Pulmonary Index (IPI) is intended for use with adult and Supported input devices include USB-compatible off-the-shelf
pediatric (1 to 12 years) patients only. The IPI is an adjunct to and not computer accessories such as a mouse, keyboard, trackball, or barcode
intended to replace vital sign monitoring. reader.
The derived measurement Pulse Pressure Variation (PPV) is intended
for use with sedated patients receiving controlled mechanical
ventilation and mainly free from cardiac arrhythmia. The PPV
measurement has been validated only for adult patients.
Modularity
The monitor’s functionality can be extended by connecting Philips
multi-measurement module family (with extensions) with plug-and-play
convenience. 1 Requires Option J15 - Adaptive Secondary Display.
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Keyboard • an additional invasive pressure measurement, a third invasive pressure
If alpha or numeric data entry is required, for example to enter patient or temperature measurement (one at a time), an integrated
demographics, a pop-up keyboard will automatically appear on the mainstream or sidestream CO2 measurement (M3014A), or
screen. If desired a USB-compatible off-the-shelf keyboard can be used • an additional invasive pressure or temperature measurement (one at
instead. a time) and a Microstream CO21 measurement (M3015A).
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• The transition from bedside monitoring to transport is smooth and • the numeric of the alarming measurement flashes on the screen.
easy, with no need to disconnect patient cables or adjust any • alarm lamps flash for red and yellow alarms and are illuminated for
measurement or monitor settings. technical INOPs.
• The monitor’s network capability means that it is ready for use as an The alarm limit review page offers an overview of alarm limit settings
integrated part of the hospital system. and the possibility to modify these settings for all parameters.
If the monitor is connected via a network to a central monitoring
Patient Transfers station, alarming is simultaneous at the monitor and at the Information
• The Universal Admit, Discharge, and Transfer (ADT) feature means Center.
that all ADT information is shared between the networked monitor • Alarms are graded and prioritized according to severity:
and the Philips IntelliVue Information Center (PIIC/PIIC iX). – Red Alarms*** identify a potentially life threatening situation for a
Information need only be entered once. patient.
• Patients can be transferred by disconnecting the MMS or X2 from a – Yellow Alarms** indicate conditions violating preset vital signs
monitor, and then reconnecting it at a new monitor. Patient limits.
demographics are stored in the MMS and the X2, so they do not have – Yellow Alarms* indicate arrhythmia alarms.
to be re-entered at the new monitor. – Technical Alarms (INOPS) are triggered by signal quality
problems, equipment malfunction, or equipment disconnect.
Patient Data Documentation • The Audio off/Pause Alarms function (equivalent to Silence/Suspend
• An extensive range of Patient Reports can be printed: with previous monitor generations) allows the user to switch off
– Event Review and Episode Reports alarm tones with one touch or click while retaining visual alarm
– 12-lead ECG Reports messages.
– Vital Signs All alarms can be paused indefinitely or for a period of 1, 2, 3, 5, or
– Graphic Trends 10 minutes depending on their configuration.
– Cardiac Output Reports Alarm strip recordings are available on the integrated recorder or on a
– Wedge Procedure Reports centrally-connected recorder.
– Calculations Reports Patented automatic alarm limits automatically adapt the alarm limits to
– Alarm Limit Reports the patient’s currently measured vital signs within a safe margin defined
– Real-time Wave Reports individually for each patient.
– Oxy CRG Reports Visual and/or audible latching and non-latching alarm handling is
Report templates can be defined in advance, enabling print-outs available.
tailored to each hospital’s specific requirements to be started quickly.
Reports can be printed on locally or centrally-connected printers, and Profiles
they can be initiated manually or automatically at user-defined intervals. Profiles are predefined configuration settings for Screens, measurement
settings, and monitor properties. Each Profile can be designed for a
Recordings specific application area and patient category, for example OR. Profiles
The integrated recorder1 records numerics for all active measurements enable a quick reaction to patient and care location changes: activating
and up to three wave forms. a Profile with a particular patient category (Adult, Pediatric or
Neonatal) automatically applies suitable alarm and safety limits and
Alarms saves time usually spent carrying out a complete set-up procedure.
The alarm system can be configured to present either the traditional Profiles can be created directly on the monitor or remotely on a
HP/Agilent/Philips alarm sounds or sounds compliant with the personal computer and transferred to the monitor using the Support
IEC 60601-1-8 Standard. Tool. A selection of Profiles for common monitoring situations is
Alarm limits are permanently visible on the main screen. When an provided with the monitor.
alarm limit is exceeded, it is signaled by the monitor in the following
ways:
• an alarm tone sounds, graded according to severity.
• an alarm message is shown on the screen, color-coded according to
severity.
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Networking Capabilities • Ventilation Calculations:
The monitor can operate as part of a networked system using the – Minute Volume (MINVOL)
Philips IntelliVue Clinical Network interface. – Compliance (COMP)
This includes: – Dead Space (Vd)
• DHCP protocol support (as an alternative to BootP in certain – Dead Space/Tidal Volume Ratio (Vd/TV)
network designs) – Alveolar Ventilation (ALVENT)
• QoS Tagging
Service Features
Other Patient Overview Capability • The Support Tool helps technical personnel to:
The alarm status of beds in the same Care Group on the hospital – carry out configuration, upgrades, and troubleshooting via the
network can be permanently displayed on the screen of each monitor network, or on an individual monitor.
in the Care Group. The user can also view measurement data from all – share configuration settings between monitors.
other monitors connected to the hospital network. Other Patient – back up the monitor settings.
information can either be viewed in a separate window or permanently – document configuration settings.
displayed on specially designed screens. • A password-protected Service Mode ensures that only trained staff
can access service tests and tasks.
Clinical Calculation Set • The Configuration Mode is password-protected and allows trained
The clinical calculation set consists of: Hemodynamic, Oxygenation, users to customize the monitor configuration.
and Ventilation calculations.
• Hemodynamic Calculations: Device Connections
– Cardiac Index (C.I.) The monitor can be connected to:
– Stroke Volume (SV) • Multi-Measurement Module (MMS) M3001A/M3001AL), and
– Stroke Index (SI) extensions (M3012A, M3014A, M3015A).
– Systemic Vascular Resistance (SVR) • Information Center (for example, PIIC iX).
– Systemic Vascular Resistance Index (SVRI)
– Pulmonary Vascular Resistance (PVR) Standard Interface Connections
– Pulmonary Vascular Resistance Index (PVRI)
– Left Cardiac Work (LCW) Adaptive Secondary Display
– Left Cardiac Work Index (LCWI) The Adaptive Secondary Display, (Option J15), activates the DVI video
– Left Ventricular Stroke Work (LVSW) interface. The output of this interface mirrors the content of the
– Left Ventricular Stroke Work Index (LVSWI) monitor display. The output supports VESA display timings allowing
– Right Cardiac Work (RCW) off-the-shelf displays to be used with the DVI output.
– Right Cardiac Work Index (RCWI)
– Right Ventricular Stroke Work (RVSW) Network Interface
– Right Ventricular Stroke Work Index (RVSWI) The network interface provides the system with networking capability
– Extra Vascular Lung Water Index (EVLWI) via a wired network connection.
– Intrathoracic Blood Volume Index (ITBVI)
– Global End Diastolic Volume Index (GEDVI) Device Interface (USB Interface)
• Oxygenation Calculations: This interface allows connection of USB devices to the monitor, for
– Arterial Oxygen Content (CaO2) example: Mouse, Keyboard, Barcode Scanner, PCL5-supported Printer.
– Venous Oxygen Content (CvO2)
– Arteriovenous Oxygen Content (CavO2) Monitor Specifications
– Oxygen Availability (DO2) For M3001A/M3001AL, X2, and MMS-extension specifications, See the
– Oxygen Availability Index (DO2I) respective Data Sheets.
– Oxygen Consumption (VO2)
– Oxygen Consumption Index (VO2I)
– Oxygen Extraction Ratio (O2ER)
– Alveolar-Arterial Oxygen Difference (AaDO2)
– Percent Arteriovenous Shunt (Qs/Qt)
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Safety Specifications Environmental Specifications
The monitors, together with the Multi-Measurement Module
(M3001A/M3001AL), the X2 Multi-Measurement Module (M3002A), MX430 Monitors
and all MMS extensions, comply with the Medical Device Directive 93/ Item Condition Range
42/EEC (CE0366) and with: Temperature Operating 0–40°C (32–100°F).
• IEC 60601-1:1988 + A1:1991 + A2:1995, Range When charging battery
• EN 60601-1:1990 + A1:1993 + A2:1995, or M3002A is mounted
• UL 60601-1:2003, on back:
• CAN/CSA C22.2#601.1-M90 + Suppl. No 1-94 + Am.2, 0–35°C (32–95°F)
• IEC 60601-1-1:2000, Storage -20–60°C (-4–140°F)
• EN 60601-1-1:2001, Humidity Operating 15–95% Relative
• IEC 60601-1-2:2001 +A1:2004, Range Humidity (RH)
• EN 60601-1-2:2001 +A1:2006. (non-condensing)
All applied parts are Type CF unless otherwise specified. They are Storage 5–95% (RH)
protected against damage from defibrillation and electrosurgery. Altitude Operating -500–3000 m (10000 ft)
The possibility of hazards arising from software errors was minimized Range Storage -500–4600 m (15000 ft)
in compliance with ISO/EN 14971 and IEC/EN60601-1-4. Ingress IP21
• This ISM device complies with Canadian ICES-001. Cet appareil ISM Protection
est conforme à la norme NMB-001 du Canada.
Performance Specifications
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MX430 Performance Specifications MX430 Performance Specifications
Trends Resolution 50 numerics with Buffered Hold Time If powered by AC:
4 h @ 12 sec, Memory infinite.
24 h @ 1 min and Without power: at
48 h @ 5 min. least 8 hours.
Events Information Trigger condition and Contents Active settings, trends,
time, event patient data, realtime
classification and reports, events, review
associated detailed alarms.
view of episode data.
Episode data Configurable, either: Interface Specifications
4 minutes of high
MX430 Interface Specifications
resolution trend or
Network Standard 10Base-T and
20 minutes of
100Base-TX (IEEE 802.3),
numerics trend @
auto-negotiation, full- and
12 sec resolution or
half-duplex
15 seconds of 4 waves
Connector RJ45 (8 pin)
@ 125 samples/sec
Isolation basic insulation:
(Snapshot) including all
reference voltage: 250 V;
current numerics,
test voltage: 1500 V
alarms and inops.
USB Standard USB 2.0 high-speed
Capacity (max.) 25 or 50 events for
Interface Connector USB series “Standard A”
either 8 or 24 hours.
receptacle
Alarm Signal System delay less than 4 seconds.
Power Low power port 4.4 V
Pause duration 1, 2, 3 minutes or
min., max. load for all
infinite, depending on
ports together 500 mA
configuration.
Isolation none
Extended alarm 5 or 10 minutes.
Video Connector DVI-I (digital single link).
pause
Interfacea Digital video single link TMDS
Review Alarms Information all alarms / inops, main
alarms on/off, alarm signals
silence and time of HSYNC/VSYNC TTL
occurrence. signals
Capacity 300 items. Vertical Frequency 59.9 Hz
Real Time Range from: January 1, 1997, Horizontal 49.3 kHz
Clock 00:00, to: Frequency
December 31, 2080, Pixel Clock 71.0 MHz ±0.5%
23:59. Resolution VESA 1280 x 800 at
Accuracy better than 4 seconds 60 Hz, reduced blanking
per day. Measurement Connectors MSL out (Proprietary)
Hold Time infinite if powered by Server Link Voltage 48 V ±10%
AC; otherwise at least (MSL) Power 12 W
48 hours Power Sync. 5 V CMOS Level,
(typical: >72 hours). 78.125 kHz (typical)
LAN signals IEEE 802.3 10-Base-T
compliant
Serial signals RS-422 compliant
ECG Sync Output/Analog ECG Output
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MX430 Interface Specifications Battery Charge Time
General Connector (1/4 in stereo phone jack • When monitor is switched off: three hours.
with tip, ring, sleeve) • When monitor is in use: up to five hours, depending on monitor
Isolation none configuration.
Battery Specifications
Interface Options
Philips high-power battery M4605A, 10.8 V 6000 mAh Lithium Ion.
• Weight: 490 g.
Wired Interfaces 866061
• Status LEDs indicate charge status of batteries.
Adaptive Secondary Display J15
• Safety: complies with UL1642 (UL recognized).
• Electromagnetic compatibility: complies with the requirements for
FCC Type B computing Device, and EN 61000-4-2 and EN 61000-4-3.
• Communication Standard: complies with the SMBus specification v1.1
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Measurement Options Related Products
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Documentation
All documentation is available in .pdf format on documentation DVD
and is shipped with the product. Additionally, a predefined number of
the Instructions for Use ships with each order.
• Instructions for Use (printed)
• Documentation DVD including:
– Installation and Service Guide
– Configuration Guide
– Quick Guides
– Application Notes
– Training Guide
Description Option #
Waves
Upgrade from 4 to 6 wavesa A06
Adaptive Secondary Display J15
a Check availability in your country.
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Philips Healthcare is part of
0366
Royal Philips
866061 complies with the requirements of
How to reach us the Council Directive 93/42/EEC of 14 June
www.healthcare.philips.com 1993 (Medical Device Directive).
healthcare@philips.com
fax: +31 40 27 64 887
Asia
+852 2821 5888
Latin America
+55 11 2125 0744
North America
+1 425 487 7000
800 285 5585 (toll free, US only)
Philips Healthcare reserves the right to make changes in specifications and/or to discontinue any product at any time without notice or
obligation and will not be liable for any consequences resulting from the use of this publication.
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